The Recall Desk

State

Missouri product recalls

73,570 recalls have nationwide distribution and so reach Missouri. 8,496 additional recalls listed Missouri specifically in their distribution scope.

What the numbers show

Total
8,496
Critical
1,344
Severe
2,198
Most recent
2026-10-14

Of the 8,496 recalls naming Missouri we have scored against our rubric, 1,344 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,198 (26%) are Severe.

Which agencies issued them

These figures cover only the 8,496 recalls whose distribution notice names Missouri specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25476–25500 of 82066

  • HighFDA (Devices)·Z-0117-2022·2021-10-20

    Beckman Coulter Power Processor 3K Recalled for Missing Splash Guard

    Beckman Coulter is recalling Power Processor 3K laboratory equipment due to a missing splash guard that may expose users to hazardous materials. Approximately 271 units were distributed in the U.S. and internationally.

    Product
    Power Processor 3K, 3K High Speed Stockyards Module Nameplate: PP 3K Stockyard (Refrig) 9707 REF A88116
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0086-2022·2021-10-20

    Endoskeleton TCS Interbody System implant engraving may not match pouch labels

    Medtronic is recalling 9 Endoskeleton TCS Interbody System surgical implants because engraving on the devices may not match the labels on the pouches. The mismatch could result in wrong devices being implanted.

    Product
    Endoskeleton" TCS Interbody System with Titan nanoLOCK" Surface Technology, NanoLock, 6 Deg, Interbody, Medium, 10mm
    Category
    Medical Device
    Distribution
    14 states
  • HighFDA (Devices)·Z-0082-2022·2021-10-20

    Bio-Rad BioPlex 2200 ANA Screen Control lot incompatible with reagents

    Bio-Rad Laboratories has recalled certain lots of BioPlex 2200 ANA Screen Control Sets due to incompatibility with older lots of ANA Screen Reagent Packs and Calibrator Sets, which may affect test accuracy.

    Product
    BioPlex 2200 ANA Screen Control Set, REF: 663-1131 incompatible with ANA Screen Reagent Packs/ANA Kits, REF: 665-1150; and ANA Screen Calibrator Sets, REF: 663-1101
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0078-2022·2021-10-20

    Philips HeartStart Defibrillator Recall: Previous Recall Notifications Not Sent

    Philips HeartStart FR2+ Defibrillators (models M3860A and M3861A) were not accompanied by notifications about previous recalls. Affected customers should contact Philips for information about prior safety issues.

    Product
    Philips, HeartStart FR2 + Defibrillator, Model # M3860A and M3861A
    Category
    Medical Device
    Distribution
    12 states
  • HighFDA (Devices)·Z-0108-2022·2021-10-20

    Evita V500 Ventilator Software Defect May Cause Temporary Ventilation Loss

    Draeger's Evita V500 ventilator software version 2.51 and lower may restart unexpectedly, briefly stopping ventilation and breathing support. 6,797 units are affected nationwide.

    Product
    Evita V500 Ventilator with Installed CO2 Measurement Option-Intended for the ventilation of adult,pediatric and neonatal patients. Catalog Number: 8416400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0081-2022·2021-10-20

    Philips HeartStart HS1 OnSite Defibrillator Recall: Notification of Previous Recalls

    Philips North America LLC is recalling 15 units of the HeartStart HS1 OnSite Defibrillator (Models M5066A and M5067A) due to failure to notify customers of previous recalls associated with these devices.

    Product
    Philips, HeartStart HS1 OnSite Defibrillator, Model #'s: M5066A and M5067A
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Devices)·Z-0080-2022·2021-10-20

    Philips HeartStart HS1 Home Defibrillator: Customers Not Notified of Previous Recalls

    Philips is recalling nine units of the HeartStart HS1 Home Defibrillator (Model M5068A) because customers were not notified of previous recalls associated with various defibrillator models.

    Product
    Philips, HeartStart HS1 Home Defibrillator, Model # Model number: M5068A
    Category
    Medical Device
    Distribution
    12 states
  • ModerateFDA (Drugs)·D-0006-2022·2021-10-20

    Potassium Chloride Extended-Release Tablets Recalled for Failed Dissolution

    Strides Pharma Inc. is recalling Potassium Chloride Extended-Release Tablets, USP 10 mEq because the tablets fail to meet dissolution specifications, which may affect drug effectiveness.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V822000·2021-10-19

    Newmar Motorhomes Power Steering Pump Defect Recall

    Newmar is recalling 2020-2022 Essex, King Aire, and London Aire motorhomes due to a power steering pump machining defect that can result in loss of steering assist and increased crash risk. Affected owners should contact Newmar for free inspection and replacement.

    Product
    NEWMAR — NEWMAR LONDON AIRE, KING AIRE, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V823000·2021-10-19

    Sutphen Fire Trucks Recalled for Excessively Bright LED Lights

    Sutphen is recalling two fire trucks because their LED lights are too bright, potentially blinding other drivers and increasing crash risk.

    Product
    SUTPHEN — SUTPHEN FIRE TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V816000·2021-10-18

    Schwarze M6 Avalanche Street Sweepers Recalled for Conveyor Hazard

    Schwarze is recalling 2012-2020 M6 Avalanche street sweepers because an outside switch box may activate unintentionally, creating a crushing hazard.

    Product
    SCHWARZE — SCHWARZE M6 AVALANCHE STREET SWEEP, M6 AVALANCHE CNG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V820000·2021-10-18

    Triple E Recreational Vehicles Recalled for Refrigerator Fire Risk

    Triple E is recalling specific 2015-2018 recreational vehicles because the refrigerator exhaust vents directly onto the wood frame, which can overheat and ignite.

    Product
    TRIPLE E — TRIPLE E, TRIPLE E RV LIBERO, WONDER, UNITY, SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V821000·2021-10-18

    2022 Mitsubishi Outlander Recalled for Defective Center Pillar Welding

    Mitsubishi is recalling one 2022 Outlander due to a welding robot error that may have caused incorrect center pillar welding, reducing crash protection. In a crash event, the reduced body strength may increase the risk of injury.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V815000·2021-10-18

    Ferrara Recalls 2021 Pumper Fire Trucks Due to Lifting Cable Defect

    Ferrara is recalling one 2021 Pumper Fire Apparatus because improperly crimped lifting cables could cause a generator set to fall, posing an injury risk.

    Product
    FERRARA — FERRARA PUMPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V818000·2021-10-18

    Mercedes-Benz Recalls Vehicles for Incorrectly Assembled Seats

    Mercedes-Benz is recalling specific 2020-2021 models because incorrectly assembled seats may not properly restrain occupants during a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLS 580 4MATIC, GLS 450, GLE 450, GLE 350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V805000·2021-10-15

    Ford vehicles recalled for damaged side impact airbag sensors

    Ford is recalling certain 2022 and 2021 model vehicles due to damaged side impact airbag sensors that may fail to deploy properly in a crash.

    Product
    FORD — FORD, LINCOLN F-150, F-350 SD, F-250 SD, EXPEDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V806000·2021-10-15

    Yamaha Recalls 2020-2021 XVS950 Motorcycles Due to Engine Oil Leak

    Yamaha is recalling 2020-2021 XVS950 motorcycles because the engine case may leak oil onto the rear tire, increasing the risk of a crash.

    Product
    YAMAHA — YAMAHA BOLT R-SPEC XVS950
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V812000·2021-10-15

    2021 Volkswagen Atlas front wheel bearing bolts may loosen and cause crash risk

    Volkswagen is recalling certain 2021 Atlas, Atlas Cross Sport, and Passat vehicles because the front wheel bearing bolts may have been incorrectly tightened and could loosen, potentially causing loss of control and crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, PASSAT, ATLAS CROSS SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V809000·2021-10-15

    2021 Ford Bronco Sport Moonroof Glass May Detach from Vehicle

    Ford is recalling certain 2021 Bronco Sport vehicles because the moonroof glass may not be bonded correctly to the frame and could detach. A detached glass panel could become a road hazard and increase crash risk.

    Product
    FORD — FORD BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide